Triampyzine

Triampyzine
Clinical data
Other names(Dimethylamino)trimethylpyrazine; W-3976B; W3976-B; W-3976-B; W3976B; 3,5,6-Trimethylampyzine
Identifiers
  • N,N,3,5,6-pentamethylpyrazin-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC9H15N3
Molar mass165.240 g·mol−1
3D model (JSmol)
  • CC1=C(N=C(C(=N1)C)N(C)C)C
  • InChI=1S/C9H15N3/c1-6-7(2)11-9(12(4)5)8(3)10-6/h1-5H3
  • Key:RKPVUWPGCFGDJO-UHFFFAOYSA-N

Triampyzine (INNTooltip International Nonproprietary Name), also known as triampyzine sulfate (USANTooltip United States Adopted Name; developmental code name W-3976B) in the case of the sulfate salt, as (dimethylamino)trimethylpyrazine, or as 3,5,6-trimethylampyzine, is a drug described as an anticholinergic and antisecretory agent which was never marketed.[1][2][3][4][5] It was first described in the literature by 1966.[1][6] The drug is the 3,5,6-trimethylated derivative of ampyzine (W-3580B), which is also a drug and is, conversely, described as a "central stimulant".[1][5][2]

References

  1. ^ a b c Elks J (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 436. ISBN 978-1-4757-2085-3. Retrieved 21 October 2024.
  2. ^ a b Milne GW (2018). Drugs: Synonyms and Properties. Routledge Revivals. Taylor & Francis. pp. 213, 547. ISBN 978-1-351-78990-5. Retrieved 21 October 2024.
  3. ^ "TRIAMPYZINE". Inxight Drugs. Retrieved 21 October 2024.
  4. ^ Negwer M (1994). Organic-chemical Drugs and Their Synonyms: (an International Survey). Akademie Verlag. p. 355. ISBN 978-3-05-500156-7. Retrieved 21 October 2024.
  5. ^ a b Lednicer D (2009). Strategies for Organic Drug Synthesis and Design. Wiley. p. 366. ISBN 978-0-470-39959-0. Retrieved 21 October 2024.
  6. ^ Marler EE (1967). Pharmacological and Chemical Synonyms: A Collection of Names of Drugs and Other Compounds Drawn from the Medical Literature of the World. Excerpta Medica. p. 322. Retrieved 21 October 2024.


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